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Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany

Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany Recalls

All product recalls associated with Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany.

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Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1101–1120 of 7756 recalls

D-Clip Applier (Peter Lazic) – Surgery Failure Risk (2023)

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

FDAOct 6, 2023Nationwide• Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany

D-Clip Applier (Peter Lazic) – Surgery Failure Risk (2023)

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

FDAOct 6, 2023Nationwide• Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany

ORION System (LEONI) – Unintended Movement Risk (2023)

Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.

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FDAOct 6, 2023Nationwide• LEONI CIA CABLE SYSTEMS 5 avenue Victor Hugo Chartres France

Favorite Day Demi French Bread (Rise Baking) – Foreign material (2023)

Foreign Material (plastic).

Class IIModerate

FDAOct 5, 2023CA, IA• Rise Baking Company, LLC dba The New French Bakery Inc.

Hillrom Progressa+ Bed (Baxter) – Static Electricity Risk (2023)

Progressa+ beds have the potential for static buildup from the casters and/or power drive. This static electricity could be passed to the operator through the transport handle during transport, resulting in a mild static electric shock.

FDAOct 4, 2023Nationwide• Baxter Healthcare Corporation

BD Insyte IV Catheter (Becton Dickinson) – Needle Retraction Issue (2023)

Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and repeat catheter insertion attempts, due to catheter being inadvertently removed from the insertion site.

FDAOct 4, 2023Nationwide• Becton Dickinson Infusion Therapy Systems Inc.

Vancomycin HCI IV Bag (Denver Solutions) – Labeling Issue (2023)

Labeling: Not Elsewhere Classified

Class IIILow

FDAOct 4, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

Vancomycin HCI IV Bag (Denver Solutions) – Labeling Issue (2023)

Labeling: Not Elsewhere Classified

Class IIILow

FDAOct 4, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

Oxytocin IV Bag (Denver Solutions) – Labeling Issue (2023)

Labeling: Not Elsewhere Classified

Class IIILow

FDAOct 4, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

GEM Premier 3000 PAK (Instrumentation) – pO2 Over-Recovery (2023)

Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications for pO2. The positive bias may lead to false positive for medical decision levels at pO2 < 60 mmHg, which may result in failure to detect and/or adequately treat hypoxemia and lead to a delay in treatment. The quality control procedures for the Non-iQM GEM Premier 3000 may not detect the non-conformance.

FDASep 29, 2023MA, MN, NY• Instrumentation Laboratory

ION*Sinus Spray (Biomic Sciences) – microbial contamination (2023)

Microbial contamination of Non-Sterile Products

Class IHigh

FDASep 29, 2023Nationwide• Biomic Sciences, LLC dba ION Intelligence of Nature

ION* Sinus Support Nasal Spray (Biomic Sciences) – microbial contamination (2023)

Microbial contamination of Non-Sterile Products

Class IIModerate

FDASep 29, 2023Nationwide• Biomic Sciences, LLC dba ION Intelligence of Nature

Restore Sinus Spray (Biomic Sciences) – microbial contamination (2023)

Microbial contamination of Non-Sterile Products

Class IIModerate

FDASep 29, 2023Nationwide• Biomic Sciences, LLC dba ION Intelligence of Nature

Zevo Flying Insect Killer (Procter & Gamble) – Injury risk (2023)

Laceration Risk

This recall involves Zevo Fly, Gnat and Fruit Fly Flying Insect Killer3 Value Packs. The twin pack aerosol containers are shrink-wrapped together with a white and purple label. The batch code 3045D185EW3 is printed on the bottom of the aerosol containers or on the shrink-wrap. "Zevo Insect Killer" and "Fly, Gnat & Fruit Fly" and "Kills on Contact" are printed on the shrink-wrap.

CPSCSep 28, 2023Nationwide• The Procter & Gamble Company, of Cincinnati, Ohio

EXALT Duodenoscope (Boston Scientific) – Image Quality Problem (2023)

Poor image quality due to fluid ingress in the lens.

FDASep 27, 2023Nationwide• Boston Scientific Corporation

Whole Cantaloupe (Martori Farms) – Salmonella Risk (2023)

Salmonella

Possible contamination with Salmonella spp.

Class IHigh

FDASep 22, 2023CA, IL, IN +17 more• Eagle Produce LLC, dba Martori Farms

Wabash National Van (Wabash National) – Lift Gate Bolts (2023)

Wabash National Corporation (Wabash) is recalling certain 2009-2024 dry van trailers equipped with a rail-style lift gate. Please see the recall report for a complete list of models. The location of the rear impact guard is too far forward from the rear of the trailer, reducing impact protection. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 224, "Rear Impact Protection."

NHTSASep 20, 2023Nationwide• WABASH NATIONAL

Nova Prime Plus Analyzer (Nova Biomedical) – Creatinine Results (2023)

Potential risk of reporting erroneous creatinine patient results associated with the initial start-up of a new BUN/Creatinine Sensor Cartridge. The potential risk is within the first 2-4 hours after cartridge installation that may not be identified by traditional Quality Control practices.

FDASep 18, 2023Nationwide• Nova Biomedical Corporation

Nova Stat Profile (Nova Biomedical) – Creatinine Results (2023)

FDASep 18, 2023Nationwide• Nova Biomedical Corporation

Nkratable Bites (The Crooked Row) – Kratom Additive (2023)

Unapproved food additive: kratom

Class IIModerate

FDASep 14, 2023TN• Cannihelp Hemp Co LLC dba The Crooked Row